Evidence map›Paper›PMID 34616846›Full record

ArticleBioMed research international2021

Comprehensive Analysis of Glutamate-Rich WD Repeat-Containing Protein 1 and Its Potential Clinical Significance for Pancancer.

Yumeng Wu, Xuming Wu, Yuanyuan Li, Wenjing Zhao, Yanping Yue, Biao Wu, Jibin Liu, Xudong Chen, Aiguo Shen

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Yumeng WuCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.ORCID https://orcid.org/0000-0001-7648-365X
Xuming WuNantong Fourth People's Hospital, China.ORCID https://orcid.org/0000-0001-7035-7513
Yuanyuan LiCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.ORCID https://orcid.org/0000-0002-6959-4682
Wenjing ZhaoCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.
Yanping YueCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.ORCID https://orcid.org/0000-0002-5059-1705
Biao WuCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.ORCID https://orcid.org/0000-0003-0182-9454
Jibin LiuCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.
Xudong ChenDepartment of Pathology, Affiliated Tumor Hospital of Nantong University, China.ORCID https://orcid.org/0000-0002-1121-8940
Aiguo ShenCancer Research Center Nantong, Affiliated Tumor Hospital of Nantong University, China.ORCID https://orcid.org/0000-0003-1821-9759
Nantong University · CNThe Fourth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

methodsThe expression level of GRWD1 in human cancer tissues was analyzed using the Tumor Immune Evaluation Resource (ver. 2.0, TIMER2), Gene Expression Profiling Interactive Analysis (ver. 2, GEPIA2), and UALCAN databases. The Kaplan-Meier plotter was utilized to analyze the survival data. Spearman's correlation analysis was used to find out the correlation between the expression level of GRWD1 and predictive biomarkers, such as tumor mutation burden (TMB) and microsatellite instability (MSI). Furthermore, the MEXPRESS website was used to study the potential relationship between DNA methylation level of GRWD1 and pathological staging. We utilized the "immune" module provided on the TIMER2 website to explore the relationship between the expression level of GRWD1 and immune infiltration in all types of cancer in TCGA. Pearson's correlation analysis was used to investigate the correlation between the expression level of GRWD1 and the expression levels of immune checkpoint-related genes. For protein expression analysis, we used the CPTAC module provided by the UALCAN portal to compare the total protein and phosphorylated protein level of GRWD1 in adjacent normal and tumor tissues.

resultsGRWD1 was overexpressed in tissues of most types of cancer, in which the expression levels of GRWD1 in the kidney chromophobe (KICH), kidney renal papillary cell carcinoma (KIRP), and kidney renal clear cell carcinoma (KIRC) tissues showed an opposite trend, and the expression level of GRWD1 was correlated to only the KIRC tumor stage. The results of survival analysis showed that the expression level of GRWD1 was significantly associated with overall survival in six types of cancer and disease-free survival (DFS) in three types of cancer. Importantly, the increased expression level of GRWD1 was strongly correlated with prognosis of KIRC patients. There was a positive relationship between the expression level of GRWD1 and immune cell infiltration in several types of cancer, and the expression level of GRWD1 was also positively correlated with TMB, MSI, and DNA methylation in some types of cancer. The results of Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis revealed that "ubiquitin mediated proteolysis," "spliceosome," and "nucleotide excision repair" were involved in the effect of GRWD1 expression on tumor pathogenesis.

conclusionThis pancancer analysis provided a comprehensive overview of the carcinogenic effects of GRWD1 on a variety of human cancers. The results of bioinformatics analysis indicated GRWD1 as a promising biomarker for detection, prognosis, and therapeutic assessment of diverse types of cancer, and GRWD1 could act as a tumor suppressor in KIRC.

Indexed as

Carrier ProteinsDNA MethylationGene Expression Regulation, NeoplasticGlutamic AcidHumansNeoplasmsPhosphorylationProtein Interaction MapsSurvival AnalysisWD40 RepeatsCarrier ProteinsGlutamic AcidGRWD1 protein, human

Identifiers

PMID34616846
PMCPMC8490071
OpenAlexW3204582243

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.